Parallel analysis of tri-molecular biosynthesis with cell identity and function in single cells

被引:24
作者
Kimmey, Samuel C. [1 ,2 ]
Borges, Luciene [2 ]
Baskar, Reema [2 ,3 ]
Bendall, Sean C. [2 ]
机构
[1] Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Pathol, Sch Med, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Canc Biol PhD Program, Stanford, CA 94305 USA
关键词
FLOW CYTOMETRIC MEASUREMENT; HEMATOPOIETIC STEM-CELLS; MASS CYTOMETRY; RNA-SYNTHESIS; PROTEIN-SYNTHESIS; DNA; TRANSLATION; PROGRESSION; IMMUNE; BROMODEOXYURIDINE;
D O I
10.1038/s41467-019-09128-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Cellular products derived from the activity of DNA, RNA, and protein synthesis collectively control cell identity and function. Yet there is little information on how these three biosynthesis activities are coordinated during transient and sparse cellular processes, such as activation and differentiation. Here, we describe Simultaneous Overview of tri-Molecule Biosynthesis (SOM3B), a molecular labeling and simultaneous detection strategy to quantify DNA, RNA, and protein synthesis in individual cells. Comprehensive interrogation of biosynthesis activities during transient cell states, such as progression through cell cycle or cellular differentiation, is achieved by partnering SOM3B with parallel quantification of select biomolecules with conjugated antibody reagents. Here, we investigate differential de novo DNA, RNA, and protein synthesis dynamics in transformed human cell lines, primary activated human immune cells, and across the healthy human hematopoietic continuum, all at a single-cell resolution.
引用
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页数:11
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